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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724496Generated: October 30, 2026

(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane → (2-Allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b']dithiophen-7-yl)dimethylsilane

https://huagongshe.com/reaction/724496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilaneHCID 21880918—
ReactantHCID 178506637HCID 178506637—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(2-Allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b']dithiophen-7-yl)dimethylsilaneHCID 21881029—

Reaction Steps

A solution of (2-allyloxy-3-tert-buyl-5-methylphenyl)chlorodimethylsilane (0.71 g, 2.40 mmol) in toluene (4 mL) was added dropwise to a solution of (2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen-7-yl)lithium (0.51 g, 2.40 mmol) in tetrahydrofuran (10 mL) at −78° C. The resulting reaction mixture was warmed to room temperature and stirred for 5 hours. After the solvent was distilled off under reduced pressure, hexane was added and the mixture was filtered to remove insoluble substances. The filtrate was concentrated under reduced pressure to quantitatively obtain (2-allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen-7-yl)dimethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141690B2
Source datasetuspto-grants-2006_11
ORD IDord-7a31c02452d54a248d81d824062fc843
Source noteuspto-grants-2006_11